Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0036305
Disease: Schamberg Disease
Schamberg Disease 		6 0 6 0.38 0 0
CUI: C1704421
Disease: Skin Pigmentation Disorder
Skin Pigmentation Disorder 		21 0 7 0.23 0 0
CUI: C0078921
Disease: Albinism, Tyrosinase-Negative
Albinism, Tyrosinase-Negative 		2 0 2 0.12 0 0
CUI: C0078922
Disease: Albinism, Tyrosinase-Positive
Albinism, Tyrosinase-Positive 		2 0 2 0.12 0 0
CUI: C0078923
Disease: Albinism, Yellow-Mutant
Albinism, Yellow-Mutant 		2 0 2 0.12 0 0
CUI: C0432315
Disease: Epidermolysis bullosa simplex herpetiformis
Epidermolysis bullosa simplex herpetiformis 		2 0 2 0.12 0 0
CUI: C0796059
Disease: Oculopalatoskeletal syndrome
Oculopalatoskeletal syndrome 		2 0 2 0.12 0 0
CUI: C1863198
Disease: ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder) 		2 0 2 0.12 0 0
CUI: C3152204
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 		2 0 2 0.12 0 0
CUI: C3715082
Disease: EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1 		2 0 2 0.12 0 0
CUI: C4302031
Disease: Basal epidermolysis bullosa simplex
Basal epidermolysis bullosa simplex 		2 0 2 0.12 0 0
CUI: C4525234
Disease: Xiphophorus Melanoma
Xiphophorus Melanoma 		2 0 2 0.12 0 0
CUI: C0268412
Disease: Infantile hypophosphatasia
Infantile hypophosphatasia 		12 0 3 0.12 0 0
CUI: C1845069
Disease: ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder) 		3 0 2 0.12 0 0
CUI: C4303860
Disease: Craniofacial ulnar renal syndrome
Craniofacial ulnar renal syndrome 		3 0 2 0.12 0 0
CUI: C0079295
Disease: Epidermolysis Bullosa Herpetiformis Dowling-Meara
Epidermolysis Bullosa Herpetiformis Dowling-Meara 		4 0 2 0.11 0 0
CUI: C0080333
Disease: Weber-Cockayne Syndrome
Weber-Cockayne Syndrome 		4 0 2 0.11 0 0
CUI: C0796032
Disease: Malpuech facial clefting syndrome
Malpuech facial clefting syndrome 		4 0 2 0.11 0 0
CUI: C0796279
Disease: Carnevale syndrome
Carnevale syndrome 		4 0 2 0.11 0 0
CUI: C1832926
Disease: EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder) 		4 0 2 0.11 0 0
CUI: C3806221
Disease: Giant melanosomes in melanocytes
Giant melanosomes in melanocytes 		4 0 2 0.11 0 0
CUI: C4024876
Disease: Palmoplantar blistering
Palmoplantar blistering 		4 0 2 0.11 0 0
CUI: C0432316
Disease: Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with mottled pigmentation 		5 0 2 0.11 0 0
CUI: C3277117
Disease: Caudal appendage
Caudal appendage 		6 0 2 1.0E-01 0 0
CUI: C4022490
Disease: Prominent coccyx
Prominent coccyx 		6 0 2 1.0E-01 0 0